E85 ICD-10-CM Code: Amyloidosis
Billing Status: NO. This is a clinician non-billable / parent hierarchy grouping in the ICD-10-CM system.
Coding at a Glance
- Tabular directives
- 5 Excludes1 · 2 Excludes2
Coding instructions
Official Tabular Instructional Notes: the inclusion, exclusion and sequencing notes published for E85 in the official ICD-10-CM tabular list, quoted as published.
Source: CMS/CDC — ICD-10-CM Tabular ListRelease: FY2026Effective: October 1, 2025
Notes without a marker are published on E85 itself; “inherited from” names the category or block whose note applies here.
Excludes1 — Not Coded Here
Conditions generally not reported together with this code (Excludes1) -- an error unless the two conditions are documented as unrelated to each other (ICD-10-CM Official Guidelines, Section I.A.12.a).
- androgen insensitivity syndrome (E34.5-) Compare E85 vs E34.5 →
- congenital adrenal hyperplasia (E25.0) Compare E85 vs E25.0 →
- hemolytic anemias attributable to enzyme disorders (D55.-) Compare E85 vs D55 →
- Marfan syndrome (Q87.4-) Compare E85 vs Q87.4 →
- 5-alpha-reductase deficiency (E29.1) Compare E85 vs E29.1 →
Source: inherited from E70-E88
Excludes2 — Not Included Here
Conditions not covered by this code, but which may be reported alongside it when both are present.
- Alzheimer's disease (G30.0-) Compare E85 vs G30.0 →
- Ehlers-Danlos syndromes (Q79.6-) inherited from E70-E88Compare E85 vs Q79.6 →
Coder workflow for E85
MedCoder structured workflow — derived from this code’s own official record
Before you code E85
- E85 is not reportable as written. Select the more specific code beneath it that the documentation supports. Codes are reported to the highest level of specificity the classification provides (Guidelines I.B.2).
ReviewE85.0, E85.1, E85.2, E85.3, E85.4, E85.8, E85.9
See the relationships section · Guide: How to choose an ICD-10-CM code →
- Check the Excludes1 note: if the documentation supports a condition named there, do not simply proceed with E85. Excludes1 conditions are not reported together with this code unless the record shows they are unrelated (Guidelines I.A.12.a).
Choose the right path
- Does the documentation support one of the more specific codes beneath E85?
Yes → Select that code and continue the checks below on its own page.
No → E85 cannot be reported as written; query for the specificity its subcategory needs. - Does the documentation support a condition named in E85’s Excludes1 note?
Yes → Do not simply proceed: review the excluded code. Both are reported only when the record shows the two conditions are unrelated.
No → Continue.
Consider E85. Then confirm the code is valid for the date of service in the Verify section.
Documentation check
- The provider’s diagnostic statement
- Codes are assigned from the provider’s documented diagnosis, not from clinical criteria, test values or a medication list (Guidelines I.A.19).
Official instructions as workflow
Excludes1 — check before selecting E85(5 notes)
Coding workflow: If the documentation supports a condition named in this note, do not simply proceed with E85: the two are not reported together. The one exception is when the record shows the two conditions are unrelated to each other.
CompareE34.5, E25.0, D55, Q87.4, E29.1
See the official tabular notes · Guidelines I.A.12.a
Excludes2 — not part of E85(2 notes)
Coding workflow: The conditions named in this note are not included in E85. When the record documents both, both may be reported; the note is a boundary, not a prohibition.
See the official tabular notes · Guidelines I.A.12.b
Coding decision scenarios
Pattern scenarios for this code’s structure — decision rules, not clinical cases
Documentation: Both the condition E85 describes and a condition named in its Excludes1 note are documented for the same encounter.
Coding question: Can both codes be reported?
Path: Review the Excludes1 note and the excluded code, and look for a provider statement on whether the two conditions are related.
Reason: Excludes1 means the two are not coded together; the exception is when the record shows the conditions are unrelated to each other (Guidelines I.A.12.a).
Every row is derived from this code’s own record — its title, tabular notes, 7th-character family and same-category siblings — with fixed MedCoder wording; nothing is inferred about a patient. The official notes and guideline text are in the sections each row links to, and they control.
Code Overview
MedCoder summary Summary composed by MedCoder from this code's official ICD-10-CM record. The tabular instructional notes themselves appear verbatim below.
Verify Before Coding
From the code registry, the Medicare Code Editor, and the MS-DRG Definitions Manual. Check it against a full claim in Claim Check.
Relationships & Classification
MedCoder structured relationships — computed from published CMS and AHRQ datasets
Other codes that name E85 or its code family, from the CMS ICD-10-CM tabular instructional notes. Tabular-note edges are stored at the code family level that carries each note.
Referenced by 7 Excludes1 notes across 3 chapters: E27.1 — Primary adrenocortical insufficiency, M60 — Myositis, M60-M63 — Disorders of muscles (M60-M63), M61 — Calcification and ossification of muscle, M62 — Other disorders of muscle, M63 — Disorders of muscle in diseases classified elsewhere, P59 — Neonatal jaundice from other and unspecified causes.
These codes’ tabular lists mark this diagnosis as mutually exclusive — not reported together unless the conditions are documented as unrelated.
Referenced by 6 Excludes2 notes across 3 chapters: G11 — Hereditary ataxia, G71 — Primary disorders of muscles, K76 — Other diseases of liver, N07 — Hereditary nephropathy, not elsewhere classified, N25.0 — Renal osteodystrophy, N25.81 — Secondary hyperparathyroidism of renal origin.
These codes’ tabular lists name this diagnosis as distinct — both may be reported when both are documented.
Referenced by 15 Code First instructions across 9 chapters: D77 — Other disorders of blood and blood-forming organs in diseases classified elsewhere, G32.8 — Other specified degenerative disorders of nervous system in diseases classified elsewhere, G63 — Polyneuropathy in diseases classified elsewhere, G99.0 — Autonomic neuropathy in diseases classified elsewhere, G99.8 — Other specified disorders of nervous system in diseases classified elsewhere, H42 — Glaucoma in diseases classified elsewhere, I43 — Cardiomyopathy in diseases classified elsewhere, I68.0 — Cerebral amyloid angiopathy, I79.8 — Other disorders of arteries, arterioles and capillaries in diseases classified elsewhere, J99 — Respiratory disorders in diseases classified elsewhere, K77 — Liver disorders in diseases classified elsewhere, L99 — Other disorders of skin and subcutaneous tissue in diseases classified elsewhere, M14.8 — Arthropathies in other specified diseases classified elsewhere, N08 — Glomerular disorders in diseases classified elsewhere, N29 — Other disorders of kidney and ureter in diseases classified elsewhere.
Each of these codes carries a Code First note naming this condition — when that code is reported, THIS code is sequenced first, ahead of it.
Contextual Map
Every relationship of E85 in one view: hierarchy, official tabular instructions in both directions, clinical classification, risk adjustment, MS-DRG participation, index terms and change history — each edge carrying the CMS source it derives from.
Run E85 with these 24 related codes in Claim Check
Hierarchy
- E00-E89 — Chapter 4: Endocrine, Nutritional and Metabolic Diseases (E00-E89) (E00-E89)[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E70-E88 — Metabolic disorders[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
Excludes1
- D55 — Anemia due to enzyme disorders[Excludes1]: “hemolytic anemias attributable to enzyme disorders (D55.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- E25.0 — Congenital adrenogenital disorders associated with enzyme deficiency[Excludes1]: “congenital adrenal hyperplasia (E25.0)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- E29.1 — Testicular hypofunction[Excludes1]: “5-alpha-reductase deficiency (E29.1)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- E34.5 — Androgen insensitivity syndrome[Excludes1]: “androgen insensitivity syndrome (E34.5-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- Q87.4 — Marfan syndrome[Excludes1]: “Marfan syndrome (Q87.4-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Excludes2
- G30.0 — Alzheimer's disease with early onset[Excludes2]: “Alzheimer's disease (G30.0-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- Q79.6 — Ehlers-Danlos syndromes[Excludes2]: “Ehlers-Danlos syndromes (Q79.6-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Referenced by Excludes1 notes
- E27.1 — Primary adrenocortical insufficiency[Excludes1]: “amyloidosis (E85.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- M60 — Myositis[Excludes1]: “myopathy in amyloidosis (E85.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- M60-M63 — Disorders of muscles (M60-M63)[Excludes1]: “myopathy in amyloidosis (E85.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- M61 — Calcification and ossification of muscle[Excludes1]: “myopathy in amyloidosis (E85.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- M62 — Other disorders of muscle[Excludes1]: “myopathy in amyloidosis (E85.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- M63 — Disorders of muscle in diseases classified elsewhere[Excludes1]: “myopathy in amyloidosis (E85.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- P59 — Neonatal jaundice from other and unspecified causes[Excludes1]: “jaundice due to inborn errors of metabolism (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Referenced by Excludes2 notes
- G11 — Hereditary ataxia[Excludes2]: “metabolic disorders (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- G71 — Primary disorders of muscles[Excludes2]: “metabolic disorders (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- K76 — Other diseases of liver[Excludes2]: “amyloid degeneration of liver (E85.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- N07 — Hereditary nephropathy, not elsewhere classified[Excludes2]: “hereditary amyloid nephropathy (E85.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- N25.0 — Renal osteodystrophy[Excludes2]: “metabolic disorders classifiable to E70-E88”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- N25.81 — Secondary hyperparathyroidism of renal origin[Excludes2]: “metabolic disorders classifiable to E70-E88”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Referenced by Code First instructions (15)
- D77 — Other disorders of blood and blood-forming organs in diseases classified elsewhere[Code First]: “amyloidosis (E85.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- G32.8 — Other specified degenerative disorders of nervous system in diseases classified elsewhere[Code First]: “amyloidosis cerebral degeneration (E85.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- G63 — Polyneuropathy in diseases classified elsewhere[Code First]: “amyloidosis (E85.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- G99.0 — Autonomic neuropathy in diseases classified elsewhere[Code First]: “amyloidosis (E85.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- G99.8 — Other specified disorders of nervous system in diseases classified elsewhere[Code First]: “amyloidosis (E85.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- H42 — Glaucoma in diseases classified elsewhere[Code First]: “amyloidosis (E85.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- I43 — Cardiomyopathy in diseases classified elsewhere[Code First]: “amyloidosis (E85.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- I68.0 — Cerebral amyloid angiopathy[Code First]: “underlying amyloidosis (E85.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- and 7 more
Nearest codes (10)
- E85.0 — Non-neuropathic heredofamilial amyloidosis[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E85.1 — Neuropathic heredofamilial amyloidosis[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E85.2 — Heredofamilial amyloidosis, unspecified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E85.3 — Secondary systemic amyloidosis[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E85.4 — Organ-limited amyloidosis[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E85.8 — Other amyloidosis[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E85.81 — Light chain (AL) amyloidosis[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E85.82 — Wild-type transthyretin-related (ATTR) amyloidosis[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- and 2 more
Change history
- FY2016 — In the code set at ICD-10-CM adoption [Change history]— CMS release files (code change ledger) · icd10cm-fy2016
Common coding questions
Can E85 be billed directly?
No. E85 (Amyloidosis) is a non-billable ICD-10-CM category code. A more specific billable subcode must be selected based on clinical documentation.
Sources for this page
Codes, titles, notes, index terms and mappings on this page are transcribed from the datasets below. Relationships MedCoder computed and text MedCoder wrote are labelled where they appear.
- Code, title, tabular notes and index terms Official source data
- CMS/CDC ICD-10-CM FY2026 tabular list, index and tables, effective October 1, 2025 Release, file and checksum · Publisher’s page
- Claim edits Official source data
- CMS Definitions of Medicare Code Edits — v43.1 (April 2026) Release, file and checksum · Publisher’s page
- Change history and date-of-service validity Official source data
- CMS ICD-10-CM release addenda, ingested release by release into the change ledger Release, file and checksum · Publisher’s page
- Comparisons, relationships and the contextual map MedCoder structured relationship
- Computed by MedCoder from the tabular notes and tables above; every derived relationship is marked as derived where it appears
- Summary and FAQ answers MedCoder explanation
- Written by MedCoder to explain the sources above: drafted with AI assistance, checked by a person against the release files, and labelled as MedCoder text where it appears. Not official text.
Labels on this page: Official source data · MedCoder structured relationship · MedCoder explanation. How to read the labels · All data sources and release dates
Cite this page
Reference this page in a research guide, syllabus or article. The release is included because code content changes each year.
MedCoder.ai. "E85 — Amyloidosis." ICD-10-CM FY2026. https://medcoder.ai/icd10/code/e85-amyloidosis
Change history
- FY2016 — October 1, 2015In the code set at ICD-10-CM adoptionAmyloidosis
No changes since FY2016 — additions, deletions, description changes and billable-status changes are tracked through FY2027 (effective October 1, 2026), and none are recorded for this code. Note changes are tracked from FY2027 only.
Nearest Codes in This Family
Official ICD-10-CM classifications closest to E85 in its code family, with their registry titles.
- E85.0 — Non-neuropathic heredofamilial amyloidosis
- E85.1 — Neuropathic heredofamilial amyloidosis
- E85.2 — Heredofamilial amyloidosis, unspecified
- E85.3 — Secondary systemic amyloidosis
- E85.4 — Organ-limited amyloidosis
- E85.8 — Other amyloidosis
- E85.81 — Light chain (AL) amyloidosis
- E85.82 — Wild-type transthyretin-related (ATTR) amyloidosis
- E85.89 — Other amyloidosis
- E85.9 — Amyloidosis, unspecified